TITANIUM SONGER CABLE SYSTEM
K-Number: K925812 · 1993-03-24
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Device Summary
Frequently Asked Questions
What is the TITANIUM SONGER CABLE SYSTEM?
TITANIUM SONGER CABLE SYSTEM is a medical device that received FDA 510(k) clearance on 1993-03-24. The listed applicant is Sofamor Danek Mfg., Inc.. The 510(k) number is K925812.
When did TITANIUM SONGER CABLE SYSTEM receive FDA 510(k) clearance?
TITANIUM SONGER CABLE SYSTEM received FDA 510(k) clearance on 1993-03-24, under 510(k) number K925812.
Who is the listed applicant for TITANIUM SONGER CABLE SYSTEM?
The FDA 510(k) record lists Sofamor Danek Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TITANIUM SONGER CABLE SYSTEM?
The FDA product code for TITANIUM SONGER CABLE SYSTEM is JDQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Sofamor Danek Mfg., Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JDQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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